Limitations to the comparative proteomic analysis of thrombopoietin producing Chinese hamster ovary cells treated with sodium butyrate

被引:30
作者
Baik, Jong Youn [1 ]
Joo, Eun Jin [2 ]
Kim, Young Hwan [2 ]
Lee, Gyun Min [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[2] Korea Basic Sci Inst, Proteom Team, Taejon 305333, South Korea
关键词
CHO cells; proteomics; serum-free culture; sodium butyrate; thrombopoietin;
D O I
10.1016/j.jbiotec.2007.11.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Sodium butyrate (NaBu) is known to enhance the specific productivity of Chinese hamster ovary cells expressing human thrombopoietin. In order to better understand the intracellular responses of these cells resulting from NaBu treatment, the proteomic profiles of cells-treated with various concentrations of NaBu (0-3 mM) were compared using two-dimensional electrophoresis (2-DE). Based on spot intensities, 80 high intensity protein spots were selected. Fifty-six of the 80 protein spots, which represent 28 different kinds of proteins, were identified by MALDI-TOF-MS and MS/MS. Compared to control without NaBu treatment, the expression levels of 2 proteins (glucose regulated protein 78 (GRP 78) and peroxiredoxin 4) were increased over two fold with NaBu treatment and the expression level of phosphopyruvate hydratase was decreased over two fold with NaBu treatment. Due to multiplicity (multiple spots for one protein), a change in one single spot intensity from a 2-DE gel image may not represent the total change in expression level for that protein. Western blot analyses of GRP78, HSC70 and ERp57 confirmed the results of the MS analyses. However, a degree of change in expression level differed between the two methods, suggesting the necessity of a validating method to determine the total amount of the protein. (C) 2007 Published by Elsevier B.V.
引用
收藏
页码:461 / 468
页数:8
相关论文
共 28 条
[1]  
Andersen DC, 2000, BIOTECHNOL BIOENG, V70, P25, DOI 10.1002/1097-0290(20001005)70:1<25::AID-BIT4>3.0.CO
[2]  
2-Q
[3]   Initial transcriptome and proteome analyses of low culture temperature-induced expression in CHO cells producing erythropoietin [J].
Baik, JY ;
Lee, MS ;
An, SR ;
Yoon, SK ;
Joo, EJ ;
Kim, YH ;
Park, HW ;
Lee, GM .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 93 (02) :361-371
[4]   BUTYRIC-ACID AND ITS MONOSACCHARIDE ESTER INDUCE APOPTOSIS IN THE HL-60 CELL-LINE [J].
CALABRESSE, C ;
VENTURINI, L ;
RONCO, G ;
VILLA, P ;
CHOMIENNE, C ;
BELPOMME, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 195 (01) :31-38
[5]   N-acetylcysteine increases the biosynthesis of recombinant EPO in apoptotic Chinese hamster ovary cells [J].
Chang, KH ;
Kim, KS ;
Kim, JH .
FREE RADICAL RESEARCH, 1999, 30 (02) :85-91
[6]  
Chung JY, 2003, J MICROBIOL BIOTECHN, V13, P759
[7]  
Eaton DL, 1997, EXP HEMATOL, V25, P1
[8]   A two-dimensional electrophoresis map of Chinese hamster ovary cell proteins based on fluorescence staining [J].
Hayduk, EJ ;
Choe, LH ;
Lee, KH .
ELECTROPHORESIS, 2004, 25 (15) :2545-2556
[9]   EFFECT OF LIPID SUPPLEMENTS ON THE PRODUCTION AND GLYCOSYLATION OF RECOMBINANT INTERFERON-GAMMA EXPRESSED IN CHO CELLS [J].
JENKINS, N ;
CASTRO, P ;
MENON, S ;
ISON, A ;
BULL, A .
CYTOTECHNOLOGY, 1994, 15 (1-3) :209-215
[10]  
Kim NS, 2001, BIOTECHNOL BIOENG, V71, P184